Midas Flowmeter; eAVS— 510(k) K241465

Name: FDA 510(k) clearance K241465
Creator: U.S. Food and Drug Administration
Published: 2024-09-19

Substantially Equivalent

Parker Hannifin Corporation

FDA 510(k) clearance K241465 for Midas Flowmeter; eAVS, Substantially Equivalent on 2024-09-19. Applicant: Parker Hannifin Corporation. Device class: 2.

Clearance details

Applicant: Parker Hannifin Corporation
Product code: Code BZR
Device class: Class 2
Regulation: 21 CFR 868.5330
Advisory panel: Anesthesiology
Date received: 2024-05-23
Decision date: 2024-09-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hatfield, PA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.